MPS I stands for Mucopolysacchardosis type I. It is an inherited genetic disorder caused by a deficiency in an enzyme called alpha-L-iduronidase (IDUA)
Learn MoreDisease management for MPS I can include supportive and symptom-based management and disease-specific management. Early intervention is important.
Learn MoreLiving with MPS I is a lifelong journey for patients and their families. Over a period of years, MPS I may present a range of challenges and experiences that may vary from individual to individual.
Learn MoreThe MPS I Registry program, sponsored and administered by Sanofi Genzyme, is a worldwide database that has been tracking health-related information for people with MPS I since 2003, allowing doctors and health care professionals to understand the disorder. Ask your doctor for more information.
Learn MoreIn this section, you’ll find valuable resources that can provide additional support and options for further learning:
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